Post Market Surveillance Specialist supporting regulatory compliance for medical devices across EU markets. Evaluate incoming complaints and maintain records in electronic database following company procedures Collect, trend, and escalate post-market surveillance data to appropriate regulatory agencies Knowledge of EU MDR 2017/745, UK Medical Devices Regulations, and Swiss Medical Devices Ordinance ~ Bachelor's degree or Swiss CFC in Health Sciences preferred ~6 months to 2 years complaint handling experience in medical devices ~ Fluent in written and spoken English, Spanish, and Portuguese ~ Attention to detail with emphasis on accuracy and data completeness ~ Proficiency with Microsoft Office suite and general computer literacy
📌 EU Post Market Surveillance Specialist (España)
🏢 Intuitive Surgical
📍 España
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